The PSIPRED Workbench is a Structural Bioinformatics service which offers a wide range of predictive methods to the bioscience community
PomBase is a model organism database that provides organization of and access to scientific data for the fission yeast Schizosaccharomyces pombe. PomBase supports genomic sequence and features, genome-wide datasets and manual literature curation.
A server to predict protein structure from sequence with facilities for variant analysis and batch processing.
From mutant genes to phenotypes! The mission of PHI-base is to provide expertly curated molecular and biological information on genes proven to affect the outcome of pathogen-host interactions. Information is also given on the target sites of some anti-infective chemistries.
LIPID MAPS® Lipidomics Gateway provide access to lipid nomenclature, databases, tools, protocols, standards, tutorials, meetings, publications, and other resources, serving the international lipid research community.
Jalview is a free program for multiple sequence alignment editing, visualisation and analysis. It allows viewing and editing of sequence alignments, their analysis with phylogenetic trees and Principal Components Analysis (PCA) plots and exploration of molecular structures and annotation. Jalview also allows integration of variant data from genome sequencing together with interactive analysis of DNA, RNA and protein sequences, phylogenetics and three-dimensional structures of macromolecules.
The IUPHAR/BPS Guide to PHARMACOLOGY is an expert-curated resource of ligand-activity-target relationships, the majority of which come from high-quality pharmacological and medicinal chemistry literature. It is a freely available, searchable database of pharmacological information that includes quantitative data on drug targets and the prescription medicines and experimental drugs that act on them.
The HUGO Gene Nomenclature Committee is the only worldwide authority that assigns standardised nomenclature to human genes.
The GWAS Central resource provides a toolkit for integrative access and visualisation of summary-level genome-wide association study data gathered from various public sources and submitted by GWAS authors, while ensuring safe open access to prevent research participant identification.
Ensembl is a genome browser for vertebrate genomes that supports research in comparative genomics, evolution, sequence variation and transcriptional regulation.